BAIT
TRP53BP1
53BP1, Tp53bp1, m53BP1, p53BP1, RP23-437L13.2
transformation related protein 53 binding protein 1
GO Process (5)
GO Function (9)
GO Component (6)
Gene Ontology Biological Process
Gene Ontology Molecular Function- RNA polymerase II activating transcription factor binding [ISO]
- RNA polymerase II transcription cofactor activity [ISO]
- damaged DNA binding [IDA]
- methylated histone binding [ISO]
- p53 binding [ISO]
- protein binding [IPI]
- sequence-specific DNA binding [IDA]
- telomeric DNA binding [IDA]
- transcription factor binding [TAS]
- RNA polymerase II activating transcription factor binding [ISO]
- RNA polymerase II transcription cofactor activity [ISO]
- damaged DNA binding [IDA]
- methylated histone binding [ISO]
- p53 binding [ISO]
- protein binding [IPI]
- sequence-specific DNA binding [IDA]
- telomeric DNA binding [IDA]
- transcription factor binding [TAS]
Gene Ontology Cellular Component
Mus musculus
PREY
TRP53
Tp53, bbl, bfy, bhy, p44, p53, RP23-56I20.1
transformation related protein 53
GO Process (100)
GO Function (32)
GO Component (17)
Gene Ontology Biological Process
- B cell lineage commitment [IMP]
- DNA damage response, signal transduction by p53 class mediator [IDA, IGI, ISO]
- DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest [IGI]
- DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator [IBA, ISO]
- DNA strand renaturation [ISO]
- ER overload response [ISO]
- T cell differentiation in thymus [IGI]
- T cell lineage commitment [IMP]
- T cell proliferation involved in immune response [IGI]
- apoptotic process [IDA, IGI]
- cell aging [IGI, ISO]
- cell cycle arrest [ISO]
- cellular protein localization [ISO]
- cellular response to DNA damage stimulus [IDA, IMP, ISO]
- cellular response to UV [IGI]
- cellular response to glucose starvation [ISO]
- cellular response to ionizing radiation [IGI, ISO]
- central nervous system development [IGI]
- cerebellum development [IDA]
- chromatin assembly [ISO]
- chromosome organization [IGI]
- determination of adult lifespan [IMP]
- double-strand break repair [IMP]
- embryo development ending in birth or egg hatching [IGI]
- embryonic organ development [IGI]
- gastrulation [IGI]
- in utero embryonic development [IGI]
- intrinsic apoptotic signaling pathway by p53 class mediator [IDA, IGI, ISO]
- intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator [IGI, IMP, ISO]
- mitochondrial DNA repair [IMP]
- mitotic G1 DNA damage checkpoint [IMP, ISO]
- mitotic cell cycle arrest [IDA]
- multicellular organism growth [IGI]
- multicellular organismal development [ISO]
- necroptotic process [IGI]
- negative regulation of DNA biosynthetic process [ISO]
- negative regulation of DNA replication [IDA, IMP]
- negative regulation of apoptotic process [IMP, ISO]
- negative regulation of cell growth [ISO]
- negative regulation of cell proliferation [IGI, IMP]
- negative regulation of fibroblast proliferation [IMP, ISO]
- negative regulation of macromitophagy [IMP]
- negative regulation of mitotic cell cycle [IGI]
- negative regulation of neuroblast proliferation [IGI]
- negative regulation of proteolysis [IMP]
- negative regulation of reactive oxygen species metabolic process [IMP]
- negative regulation of smooth muscle cell proliferation [ISO]
- negative regulation of transcription from RNA polymerase II promoter [IDA, IGI, IMP, ISO]
- negative regulation of transcription, DNA-templated [IMP, ISO]
- negative regulation of transforming growth factor beta receptor signaling pathway [IMP]
- neuron apoptotic process [IGI, IMP]
- nucleotide-excision repair [ISO]
- oligodendrocyte apoptotic process [ISO]
- oxidative stress-induced premature senescence [ISO]
- positive regulation of apoptotic process [IGI, IMP, ISO]
- positive regulation of cardiac muscle cell apoptotic process [IMP]
- positive regulation of cell aging [IMP]
- positive regulation of cell cycle [ISO]
- positive regulation of cell cycle arrest [ISO]
- positive regulation of histone deacetylation [IDA]
- positive regulation of intrinsic apoptotic signaling pathway [ISO]
- positive regulation of leukocyte migration [ISO]
- positive regulation of mitochondrial membrane permeability [IGI]
- positive regulation of neuron apoptotic process [IDA, IGI, IMP]
- positive regulation of peptidyl-tyrosine phosphorylation [IMP]
- positive regulation of protein oligomerization [ISO]
- positive regulation of reactive oxygen species metabolic process [ISO]
- positive regulation of release of cytochrome c from mitochondria [ISO]
- positive regulation of thymocyte apoptotic process [IMP]
- positive regulation of transcription from RNA polymerase II promoter [IBA, IDA, IGI, IMP, ISO]
- positive regulation of transcription, DNA-templated [IDA, IGI, ISO]
- protein complex assembly [ISO]
- protein import into nucleus, translocation [IDA]
- protein localization [ISO]
- rRNA transcription [IGI]
- regulation of apoptotic process [ISO]
- regulation of catalytic activity [IDA]
- regulation of cell cycle [IGI, IMP]
- regulation of cell proliferation [IGI, IMP]
- regulation of fibroblast apoptotic process [IGI]
- regulation of intracellular pH [ISO]
- regulation of intrinsic apoptotic signaling pathway by p53 class mediator [IMP]
- regulation of mitochondrial membrane permeability involved in apoptotic process [IGI]
- regulation of neuron apoptotic process [IGI]
- regulation of thymocyte apoptotic process [IGI]
- regulation of tissue remodeling [IMP]
- regulation of transcription from RNA polymerase II promoter [IDA]
- regulation of transcription, DNA-templated [IDA, ISO]
- release of cytochrome c from mitochondria [IDA, IGI]
- replicative senescence [ISO]
- response to UV [IDA, IMP]
- response to X-ray [IDA]
- response to drug [IDA]
- response to gamma radiation [IDA, IMP, ISO]
- response to ischemia [IMP]
- response to oxidative stress [IGI, IMP]
- response to salt stress [IGI]
- somitogenesis [IGI]
- transcription from RNA polymerase II promoter [IGI]
- transforming growth factor beta receptor signaling pathway [IGI]
Gene Ontology Molecular Function- ATP binding [ISO]
- DNA binding [IDA, ISO]
- MDM2/MDM4 family protein binding [IPI, ISO]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription [IDA, IGI]
- RNA polymerase II core promoter sequence-specific DNA binding [IDA]
- RNA polymerase II transcription factor binding [ISO]
- RNA polymerase II transcription regulatory region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription [ISO]
- chaperone binding [ISO]
- chromatin binding [IDA, ISO]
- copper ion binding [ISO]
- damaged DNA binding [IBA]
- double-stranded DNA binding [IBA]
- enzyme binding [ISO]
- histone acetyltransferase binding [ISO]
- histone deacetylase regulator activity [IDA]
- identical protein binding [ISO]
- p53 binding [IBA]
- protease binding [ISO]
- protein C-terminus binding [ISO]
- protein N-terminus binding [ISO]
- protein binding [IPI]
- protein heterodimerization activity [ISO]
- protein kinase binding [ISO]
- protein phosphatase 2A binding [ISO]
- protein phosphatase binding [ISO]
- receptor tyrosine kinase binding [ISO]
- sequence-specific DNA binding [IBA, ISO]
- sequence-specific DNA binding transcription factor activity [IDA, ISO]
- transcription cofactor binding [ISO]
- transcription factor binding [ISO]
- transcription regulatory region DNA binding [ISO]
- ubiquitin protein ligase binding [ISO]
- ATP binding [ISO]
- DNA binding [IDA, ISO]
- MDM2/MDM4 family protein binding [IPI, ISO]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription [IDA, IGI]
- RNA polymerase II core promoter sequence-specific DNA binding [IDA]
- RNA polymerase II transcription factor binding [ISO]
- RNA polymerase II transcription regulatory region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription [ISO]
- chaperone binding [ISO]
- chromatin binding [IDA, ISO]
- copper ion binding [ISO]
- damaged DNA binding [IBA]
- double-stranded DNA binding [IBA]
- enzyme binding [ISO]
- histone acetyltransferase binding [ISO]
- histone deacetylase regulator activity [IDA]
- identical protein binding [ISO]
- p53 binding [IBA]
- protease binding [ISO]
- protein C-terminus binding [ISO]
- protein N-terminus binding [ISO]
- protein binding [IPI]
- protein heterodimerization activity [ISO]
- protein kinase binding [ISO]
- protein phosphatase 2A binding [ISO]
- protein phosphatase binding [ISO]
- receptor tyrosine kinase binding [ISO]
- sequence-specific DNA binding [IBA, ISO]
- sequence-specific DNA binding transcription factor activity [IDA, ISO]
- transcription cofactor binding [ISO]
- transcription factor binding [ISO]
- transcription regulatory region DNA binding [ISO]
- ubiquitin protein ligase binding [ISO]
Gene Ontology Cellular Component
- PML body [ISO]
- chromatin [IBA, ISO]
- cytoplasm [IDA, ISO]
- cytosol [IDA, ISO]
- intracellular [IGI]
- mitochondrial matrix [IDA]
- mitochondrion [IBA, IDA, IGI, ISO]
- nuclear body [ISO]
- nuclear chromatin [ISO]
- nuclear matrix [ISO]
- nucleolus [ISO]
- nucleoplasm [ISO]
- nucleus [IDA, ISO]
- protein complex [ISO]
- replication fork [IDA]
- transcription factor TFIID complex [ISO]
- transcription factor complex [IBA, ISO]
Mus musculus
Phenotypic Enhancement
A genetic interaction is inferred when mutation or overexpression of one gene results in enhancement of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene.
Publication
53BP1 facilitates long-range DNA end-joining during V(D)J recombination.
Variable, diversity and joining (V(D)J) recombination and class-switch recombination use overlapping but distinct non-homologous end joining pathways to repair DNA double-strand-break intermediates. 53BP1 is a DNA-damage-response protein that is rapidly recruited to sites of chromosomal double-strand breaks, where it seems to function in a subset of ataxia telangiectasia mutated (ATM) kinase-, H2A histone family member X (H2AX, also known as ... [more]
Nature Nov. 27, 2008; 456(7221);529-33 [Pubmed: 18931658]
Throughput
- Low Throughput
Ontology Terms
- phenotype: absent lymphocyte (MP:0000726) [absent lymphocyte (MP:0000726)]
Additional Notes
- figure 1a. double mutant enhanced the aberrant levels of T-cell antigen receptor (TCR)-a observed in single mutants.
Curated By
- BioGRID